Canonical Allele Identifier:
CA2129379058
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36384882C= , CM000676.2:g.36384882C= | GRCh38 |
| NC_000014.8:g.36854087C= , CM000676.1:g.36854087C= | GRCh37 |
| NC_000014.7:g.35923838C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537428.1:c.319-12277C= | XP_011535730.1:n.319-12277C= | |
| XR_943756.1:n.358+23786C= |